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Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Minoxidil and Finasteride are effective for male baldness; more research is needed for hair aging treatments.

Bioengineering can potentially treat hair loss by regenerating hair follicles and cloning hair, but the process is complex and needs more research.

Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

The convention discussed various skin conditions and treatments, and highlighted the importance of vaccinations for patients on immune-altering medications.

Dihydrotestosterone and 5α-Reductase play a role in hair loss and prostate health, and finasteride can increase hair growth in men without affecting sperm production, but it doesn't work for postmenopausal women with hair loss.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

A condition called Central Centrifugal Cicatricial Alopecia causes hair loss and scalp burning in middle-aged African women, and it's treated with various medications, hair transplants, and non-drug methods like wigs.

Only a few hair-specific keratins are linked to inherited hair disorders.

PCOS is a condition causing irregular periods, excess male hormones, and infertility, often managed by targeting insulin resistance and specific symptoms.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The study found that specific proteins are markers of hair follicle development in human fetuses.

Exosome treatment safely increases hair density in male patients with androgenetic alopecia.

Hair loss in middle-aged women is often linked to insulin resistance and a family history of hair loss, particularly from their fathers.

Caffeine may help hair growth in hereditary hair loss.

Mutations in the KRT85 gene cause hair and nail problems.

Hair loss is caused by genetics and hormones, diagnosed through examination and biopsy, and treated with medications or surgery.

Most treatments for hair loss in 1997 were not effective for most people, and maintaining hair growth was difficult.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Mutation in hairless gene may increase hair loss risk.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Mutation in hairless gene may increase hair loss risk.